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Thionyl Chloride → HCID 19813434, 화합물

HRID 1031974
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HRID 1031974 반응식
S(Cl)([Cl:3])=O.O[CH2:6][C:7]1[O:8][C:9]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:10]=2[C:11]=1[CH3:12]>C(Cl)Cl.N1C=CC=CC=1.O>[Cl:3][CH2:6][C:7]1[O:8][C:9]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][C:10]=2[C:11]=1[CH3:12]
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참가 물질

6

반응물 2

HCID 24386Thionyl ChlorideHCID 19813433HCID 19813433, 화합물

생성물 1

HCID 19813434HCID 19813434, 화합물

시약·촉매·용매 3

HCID 1049Pyridine촉매HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

Thionyl chloride (1.48 g, 12.4 mmole) was added dropwise to a solution of 2-hydroxymethyl-3-methyl-5-nitrobenzofuran (0.86 g, 4.15 mmole) in methylene chloride (10 ml) and pyridine (2 drops) and the mixture was stirred at room temperature for 24 hours. The reaction mixture was then diluted with water, the organic phase separated, and the aqueous phase re-extracted with methylene chloride. The combined organic phases were washed with aqueous sodium bicarbonate, dried (Na2SO4) and the solvent evaporated to leave the title compound, 0.93 g. A portion was recrystallised from ethanol, m.p. 141°-142°.

후처리

  1. customthe organic phase separated
  2. extractionthe aqueous phase re-extracted with methylene chloride
  3. washThe combined organic phases were washed with aqueous sodium bicarbonate
  4. dry with materialdried (Na2SO4)
  5. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-ca54a74d83be4f3898e0c2945b2388f9
출처 데이터셋
uspto-grants-1990_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04956382

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